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rs74085882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs74085882(C;C)
Make rs74085882(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position51944251
GeneATP7B
is asnp
is mentioned by
dbSNPrs74085882
ebirs74085882
HLIrs74085882
Exacrs74085882
Varsomers74085882
Maprs74085882
PheGenIrs74085882
hapmaprs74085882
1000 genomesrs74085882
hgdprs74085882
ensemblrs74085882
gopubmedrs74085882
geneviewrs74085882
scholarrs74085882
googlers74085882
pharmgkbrs74085882
gwascentralrs74085882
openSNPrs74085882
23andMers74085882
23andMe allrs74085882
SNP Nexus

SNPshotrs74085882
SNPdbers74085882
MSV3drs74085882
GWAS Ctlgrs74085882
GMAF0.001377
Max Magnitude0
ClinVar
Risk rs74085882(C;C)
Alt rs74085882(C;C)
Reference rs74085882(T;T)
Significance Other
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52518387T>C
CLNSRC ClinVar LabCorp University of Washington
CLNACC RCV000029368.3,